Canonical Allele Identifier: CA2643090593
Gene: CA6 HGNC NCBI

Linked Data

gnomAD v4: 1-8957065-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8957065A>C , CM000663.2:g.8957065A>C GRCh38
NC_000001.10:g.9017124A>C , CM000663.1:g.9017124A>C GRCh37
NC_000001.9:g.8939711A>C NCBI36
NG_033975.1:g.16232A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377443.7:c.260-72A>C MANE Select ENSP00000366662.2:n.260-72A>C
ENST00000377436.6:c.260-72A>C ENSP00000366654.3:n.260-72A>C
ENST00000377442.3:c.80-72A>C ENSP00000366661.2:n.80-72A>C
ENST00000377443.6:c.260-72A>C ENSP00000366662.2:n.260-72A>C
ENST00000476083.1:n.99-1845A>C
ENST00000549778.5:c.169-77A>C ENSP00000447108.1:n.169-77A>C
NM_001215.3:c.260-72A>C NP_001206.2:n.260-72A>C
NM_001270500.1:c.260-72A>C NP_001257429.1:n.260-72A>C
NM_001270501.1:c.80-72A>C NP_001257430.1:n.80-72A>C
NM_001270502.1:c.25-1845A>C NP_001257431.1:n.25-1845A>C
XM_011542083.1:c.272-72A>C XP_011540385.1:n.272-72A>C
XM_011542084.1:c.272-72A>C XP_011540386.1:n.272-72A>C
XM_011542083.3:c.272-72A>C XP_011540385.1:n.272-72A>C
XM_011542084.3:c.272-72A>C XP_011540386.1:n.272-72A>C
NM_001215.4:c.260-72A>C MANE Select NP_001206.2:n.260-72A>C
NM_001270500.2:c.260-72A>C NP_001257429.1:n.260-72A>C
NM_001270501.2:c.80-72A>C NP_001257430.1:n.80-72A>C
NM_001270502.2:c.25-1845A>C NP_001257431.1:n.25-1845A>C